Abstract
Purpose
The purpose of this study was to examine how men without partners make decisions about prostate cancer treatment, manage treatment side effects, and obtain information and support.
Background
In 2009, it was projected that over 230,000 men were diagnosed with prostate cancer. While treatment options vary, these options result in changes within the man that can affect his quality of life. Research has shown that often spouses play a central role in men’s choice of treatment and in maintaining men’s quality of life. In addition, spouses are the major providers of emotional support and physical care. However, little is known about how men without partners cope with prostate cancer. Prior research seldom addresses how diagnosis and treatment for prostate cancer affects the quality of life of men without partners.
Methods
Because very little is known about the needs of men without partners managing prostate cancer, qualitative analysis of data obtained during semi-structure interviews provided respondents with an opportunity to share the lived experience of prostate cancer. A semi-structured interview was conducted with selected, consenting men. The sample was drawn from the ongoing R01 study of men with prostate cancer (PROSTQA).
Results
The sample for this study included 17 unpartnered prostate cancer survivors. The ages of participants ranged from 47 to 72 with a mean age of 63. The participants had between zero and two co-morbidities with an average of one co-morbidity per participant. The sample was 82% Caucasian and 17% Black. A total of 35% of the participants reported “some college” (n = 6), 30% graduated from college (n = 5), and 23% went to graduate school (n = 4). One participant reported that he was a high school graduate and one had less than a high school education. Five themes emerged from the data: going it alone, diagnosis and prostate cancer treatment decision-making, sources of information and support, the aftermath of prostate cancer, and coping strategies.
Conclusions
This study provides information about unpartnered men’s prostate cancer experience. This information will help health care professionals to meet the needs of unpartnered more effectively and help them to assist men as they adapt to living with this chronic illness.
Similar content being viewed by others
References
Jemal A, Siegel R, Ward E, Hao Y, Xu J, Murray T, et al. Cancer statistics. CA Cancer J Clin. 2009;59(4):225–49.
Litwin MS, Sadetsky N, Pasta DJ, Lubeck DP. Bowel function and bother after treatment for early stage prostate cancer: a longitudinal quality of life analysis from CaPSURE. J Urol. 2004;172:515–9.
Hu JC, Elkin EP, Pasta DJ, Lubeck DP, Katttan MW, Carroll PR, et al. Predicting quality of life after radical prostatectomy: results from CaPSURE. J Urol. 2004;171:703–8.
Hedestig O, Sandman P, Tomic R, Widmark A. Living after external beam radiotherapy of localized prostate cancer. Cancer Nurs. 2005;28(4):310–7.
Ward-Smith P, Kapitan D. Quality of life among men treated with radiation therapy for prostate cancer. Urol Nurs. 2005;25(4):263–8.
Novan L, Morag A. Advanced prostate cancer patients’ relationships with their spouses following hormonal therapy. Eur J Oncol Nurs. 2003;7:73–80.
Harden J, Schafenacker A, Northouse LL, Mood D, Smith D, Pienta K, et al. Couples’ experiences with prostate cancer: focus group research. Oncol Nurs Forum. 2002;29(4):701–9.
Harden J, Northouse LL, Mood D. Qualitative analysis of couples’ experience with prostate cancer by age cohort. Cancer Nurs. 2006;29(5):367–77.
Maliski SL, Heilemann MV, McCorkle R. From “death sentence” to “good cancer”: couples’ transformation of a prostate cancer diagnosis. Nurs Res. 2002;51(6):391–7.
Jakobsson L, Hallberg IR, Loven L. Experiences of daily life and life quality in men with prostate cancer: an exploratory study. Part 1. Eur J Cancer Care. 1997;6:108–11.
National Cancer Institute. Prostate Cancer Progress Report. 2004. Washington: Author. Retrieved from http://planning.cancer.gov/library/2004prostateProgRpt.pdf
National Cancer Institute. Prostate cancer research plan FY 2003-2008. 2002. Washington: Author. Retrieved from http://planning.cancer.gov/pdfprgreports/prostateplan.pdf
Krongrad A, Lai H, Burke MA, Goodkin K, Lai S. Marriage and mortality in prostate cancer. J Urol. 1996;156(5):1696–1700.
Denberg TD, Beaty BL, Kim FJ, Steiner JF. Marriage and ethnicity predict treatment in localized prostate carcinoma. Cancer. 2005;103(9):1819–25.
Perczek RE, Burke MA, Carver CS, Krongrad A, Terris MK. Facing a prostate cancer diagnosis: who is at risk for increased distress? Cancer. 2002;94(11):2923–9.
Sanda MG, Dunn RL, Michalski J, Sandler HM, Northouse L, Hembroff L, et al. Quality of life and satisfaction with outcome among prostate-cancer survivors. N Engl J Med. 2008;358(12):1250–61.
Newell GR, Pollack ES, Spitz MR, Sider JG, Fueger JJ. Incidence of prostate cancer and marital status. J Natl Cancer Inst. 1987;79(2):259–62.
Vaartio H, Kivineimi K, Suominen T. Men’s experiences and their resources from cancer diagnosis to recovery. Eur J Oncol Nurs. 2003;7(3):182–90. doi:10.1016/S1462-3889(03)00006-1.
Korfage IJ, de Koning HJ, Roobol M, Schroder FH, Essink-Bot ML. Prostate cancer diagnosis: the impact on patients’ mental health. Eur J Cancer. 2006;42(2):165–70.
Ben-Tovim DI, Dougherty MLG, Stapleton AMF, Pinnock CB. Coping with prostate cancer: a quantitative analysis using a new instrument, the centre for clinical excellence in urological research coping with cancer instrument. Urology. 2002;59(3):383–8. doi:10.1016/S0090-4295(01)01540-0.
Thaxton L, Emshoff JG, Guessous O. Prostate cancer support groups: literature review. J Psychosoc Oncol. 2005;23(1):25–40.
Connell RW, Messerschmidt JW. Hegemonic masculinity: Rethinking the concept. Gend Soc. 2005;19(6):829–59. doi:10.1177/0891243205278639.
Crighton FL. University Kansas research paper. 2002. p. 165.
Harden J, Schafenacker A, Northouse L, Mood D, Pienta K, Hussain M, et al. Couples experiences with prostate cancer: focus group research. Oncol Nurs Forum. 2002;29:701–9.
Lintz K, Moynihan C, Steginga S, Norman A, Eeles K, Huddart R, Dearnaley D, Watson NM. Prostate cancer patient’s support and psychological care needs: Survey from a Non-Surgical Oncology Clinic. 2002; 50
Wallace M, Storms S. The needs of men with prostate cancer. Appl Nurs Res. 2007;20(4):181–7.
Robinson A, Thomson R. Variability in patient preferences for participating in medical decision making: implication for the use of decision support tools. Qual Health Care. 2001;10 Suppl 1:34–8.
Whitney SN, McGuire AL, McCullough LB. A typology of shared decision making, informed consent, and simple consent. Ann Intern Med. 2004;140:54–9.
American Urological Association. Prostate specific antigen best practice statement. 2009. Retrieved June 29, 2009 from http://www.auanet.org/content/guidelines-and-quality-care/clinical-guidelines/main-reports/psa09.pdf.
Schröder FH, Hugosson J, Roobol MJ, Tammela TL, Ciatto S, Nelen V, et al. Screening and prostate-cancer mortality in a randomized European study. N Engl J Med. 2009;360(13):1320–8.
Pew Internet & American Life Project. Seeding the cloud: what mobile access means for usage patterns and online content. 2008. Retrieved September 20, 2008. From http://www.pewinternet.org/pdfs/PIP_Users.and.Cloud.pdf.
Broom A. The eMale: prostate cancer, masculinity and online support as a challenge to medical expertise. J Sociol. 2005;41(1):87–104.
Smither AR, Guralnick ML, Davis NB, See WA. Quantifying the natural history of post-radical prostatectomy incontinence using objective pad test data. BMC Urology. 2007; 7(2)
Siegel T, Moul JW, Spevak M, Alvord WG, Costabile RA. The development of erectile dysfunction in men treated for prostate cancer. J Urol. 2001;165(2):430–5.
Yoshioka Y. Current status and perspectives of brachytherapy for prostate cancer. Int J Clin Oncol. 2009;14:31–6.
Lazarus RS. Coping theory and research: past, present, and future. Psychosom Med. 1993;55(3):234–47.
Link LB, Robbins L, Mancuso CA, Charlson ME. How do cancer patients choose their coping strategies? A qualitative study. Patient Education and Counseling 2005 58(1), 96–103. Retrieved from http://dx.doi.org/10.1016/j.pec.2004.07.007
PROSTQA Consortium study group
The PROSTQA Consortium includes contributions in cohort design, patient accrual and follow-up from the following faculty: John T. Wei, Rodney L Dunn, and David Wood (University of Michigan); Eric A Klein and Jay Ciezki (Cleveland Clinic); Jeff Michalski and Adam Kibel (Washington University, St. Louis, WA); Mark Litwin and Chris Saigal (University of California—Los Angeles Medical Center, Los Angeles, CA); Louis Pisters and Deborah Kuban (MD Anderson Cancer Center, Houston, TX); James Hu (Brigham and Women’s Hospital, Boston, MA) Douglas Dahl and Anthony Zeitman (Massachusetts General Hospital, Boston, MA), Irving Kaplan (Beth Israel Deaconess Medical Center, Boston, MA and), Howard M. Sandler (Cedars-Sinai Medical Center, Los Angeles, CA) and Larry Hembroff (Michigan State University, East Lansging, MI)
Funding
NIH R01 CA95662
Author information
Authors and Affiliations
Consortia
Corresponding author
Rights and permissions
About this article
Cite this article
Kazer, M.W., Harden, J., Burke, M. et al. The experiences of unpartnered men with prostate cancer: a qualitative analysis. J Cancer Surviv 5, 132–141 (2011). https://doi.org/10.1007/s11764-010-0157-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11764-010-0157-3